510(k) K933391 ยท DYF Prosthesis, Vascular Graft, Of Less Then 6mm Diameter
ATRIUM'S HYBRID PTFE
| Applicant | Atrium Medical Corp., Hollis NH, US |
| Decision | Unknown, Dec 15, 1994 |
| Received | Jul 12, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K933391
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.